S. Petrović, N. Andjelic, M. Popović, B. Nikolin, Natasa Prvulovic-Bunovic
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引用次数: 0
摘要
介绍。未分化多形性肉瘤,以前称为恶性纤维组织细胞瘤,是成人中最常见的软组织肉瘤,腹膜后是第二常见的位置。病例报告。我们提出一个病例60岁的女性患者的无痛性肿块在左腹部。计算机断层扫描显示清晰的腹膜后肿块,而磁共振在t1加权上显示分叶状低密度肿块,t2加权上显示不均匀肿块,大小为180 x 230 x 250 mm,周围增强强烈。患者全部切除肿瘤,局部复发后再次手术。经手术材料的组织病理学和免疫组织化学分析,诊断为恶性纤维组织细胞瘤(巨细胞型)。结论。影像学对未分化多形性肉瘤的诊断准确性有限,最终诊断依赖于组织病理学证实。
Undifferentiated pleomorphic retroperitoneal sarcoma: A case report
Introduction. Undifferentiated pleomorphic sarcoma, previously known as malignant fibrous histiocytoma, is the most common soft tissue sarcoma in adults, and retroperitoneum is the second most common location. Case Report. We present a case of a 60-year-old female patient with a painless mass in the left hemiabdomen. Computed tomography revealed a well defined retroperitoneal mass, while magnetic resonance showed a lobulated hypointense mass on T1-weighted and heterogeneous on T2-weighted images 180 x 230 x 250 mm in size, with intense peripheral enhancement. The patient underwent complete tumor excision, as well as reoperation after local recurrence. After histopathological and immunohistochemical analysis of the operating material, the diagnosis of malignant fibrous histiocytoma (giant cell type) was made. Conclusion. Radiological imaging has a limited diagnostic accuracy in undifferentiated pleomorphic sarcomas and definitive diagnosis relies on histopathological confirmation.